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NEONATAL JAUNDICE
DR FARAH HASSAN
HOUSE OFFICER PEADIATRICS
NEONATAL JAUNDICE
 Yellowish discolouration of skin, sclera and
mucosa.
 Increase concentration of bilirubin in the
blood.
INCIDENCE
 60% of term infants
 80% of preterm infants
PHOTOTHERAPY
 PRINICIPLE
. Bilirubin absorb visible light in the blue
region(420- 490nm)and convert fat soluble
unconjugated bilirubin into non-toxic ,water-soluble
form by photo-isomerization and photo-oxidation and
excreted in bile and urine.
SIDE EFFECT
 Loose stools
 Hypothermia or hyperthermia
 Rashes
 Dehydration
 Damage to exposed eyes and genitelia
 Bronze baby syndrome with conjugated
hyperbilirubinemia phototherapy causes photo
destruction of copper porphyries cause urine and skin to
become bronze in colour.
Phototherapy Rash
EXCHANGE TRANSFUSION
 It is a procedure in which the patient’s blood is
exchanged with a donor blood, blood components and
fluids in order to remove abnormal blood or toxins
• TYPES:
Partial ET
Single volume ET
Double volume ET
INDICATIONS
 • HYPERBILIRUBINEMIA

 • SEPSIS

 • SEVERE ANEMIA

 • POLYCYTHEMIA

 • SICKLE CELL ANEMIA

 • DIC

 • HYDROPS FETALIS

 • POISINING
ACCESS
 CENTRAL VIA THE UMBLICAL VEIN

 • PERIPHERAL VIA PERIPHERAL VEIN
BLOOD TEST PRIOR TO
EXCHANGE
 BIOCHEMISTRY
 FULL SEPTIC WORKUP
 ON CORD BLOOD:
 DIRECT COOMBS TEST
 HB
 SERUM BILIRUBIN
 ON BABYS BLOOD.
 ABO, RH FACTOR, DIRECT COOMBS TEST
TYPES OF BLOOD NEEDED
 • O Rh –ive blood is used

 • If available before delivery, cross match against mothers blood

 • If obtained after delivery ,cross match with infants blood
AMOUNT OF BLOOD FOR
DOUBLE EXCHANGE
 85* wt *2

 This removes 85% of infants rbcs

 At end of exchange bilirubin should be about 50% of pre

 exchange level
BASELINE OBSERVATION
 • Vital signs

 • Blood sugar level

 • Abdominal girth measurement to evaluate haemorrhage

 • Urine analysis

 • Infants color tone activity
PRINCIPLES
 Carried through a catheter using a three way cannula
 Blood is drawn out of baby 5-20ml and discarded
down outflow line
 Aliquots 5ml for 1kg, 10ml for 2kg,, 15ml for 3kg,
>3kg 20ml cycles
 Donor blood is warmed drawn into a syringe and
injection slowly.
PRINCIPAL
 App 100ml/ 15min should be exchanged
 Record exact amount of blood exchanged
 Equal volumes exchanged in and out
 Vital signs recorded every 15 mins
RISK DURING EXCHANGE
 Blood overload congestive heart failure
 Insufficient blood anaemia
 Perforation with catheter
 Air or blood embolism
COMPLICATION
 Infection
 Haemorrhage
 Anaemia
 Trauma to vessels
 Arrhythmia and cardiac failure
 Hypotension and shock
 Electrolyte imbalance
 Graft vs host disease
VIDEO
PHARMACOLOGICAL THERAPY
 Phenobarbital
 Action:
Induce production of glucoronyltransferase and
Increase bilirubin excretion
 Indication:
CNJ II syndrome and Gilbert syndrome
 Dose:
2.5 mg/kg/day
 Metalloporphyrins
Synthetic heme ,inhibit heme oxygenase thus decrease
the production of bilirubin
PHARMACOLOGICAL THERAPY
 Intravenous Albumin
Given 1g/kg over 2 hours can provide more
binding sites for free bilirubin
 Iv immunoglobulin
Block fc receptors in neonatal reticuloendothelial system
and prevent further haemolysis is recommended if TSB
is rising despite intensive phototherapy
 Dose:500mg -1g/kg over 2hours
 Repeated after 12 hours
MANAGEMENT OF CONJUGATED
BILIRUBIN
 MEDICAL MANAGEMENT
 Antibiotics (sepsis, UTI)
 L-thyroxin (hypothyroidism)
 Hormone replacement therapy
 Vitamins
 Dietary restriction
PHARMACOLOGICAL THERAPY
 Ursodiol
 20 mg /kg /day in 2 divided doses
 Phenobarbital
 3-5mg/kg /day
 Cholestyramin
 Surgical management

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neonatal hyperbilirubinemia Presentation (3).pptx

  • 1. NEONATAL JAUNDICE DR FARAH HASSAN HOUSE OFFICER PEADIATRICS
  • 2. NEONATAL JAUNDICE  Yellowish discolouration of skin, sclera and mucosa.  Increase concentration of bilirubin in the blood.
  • 3. INCIDENCE  60% of term infants  80% of preterm infants
  • 4. PHOTOTHERAPY  PRINICIPLE . Bilirubin absorb visible light in the blue region(420- 490nm)and convert fat soluble unconjugated bilirubin into non-toxic ,water-soluble form by photo-isomerization and photo-oxidation and excreted in bile and urine.
  • 5.
  • 6.
  • 7. SIDE EFFECT  Loose stools  Hypothermia or hyperthermia  Rashes  Dehydration  Damage to exposed eyes and genitelia  Bronze baby syndrome with conjugated hyperbilirubinemia phototherapy causes photo destruction of copper porphyries cause urine and skin to become bronze in colour.
  • 9. EXCHANGE TRANSFUSION  It is a procedure in which the patient’s blood is exchanged with a donor blood, blood components and fluids in order to remove abnormal blood or toxins • TYPES: Partial ET Single volume ET Double volume ET
  • 10. INDICATIONS  • HYPERBILIRUBINEMIA   • SEPSIS   • SEVERE ANEMIA   • POLYCYTHEMIA   • SICKLE CELL ANEMIA   • DIC   • HYDROPS FETALIS   • POISINING
  • 11. ACCESS  CENTRAL VIA THE UMBLICAL VEIN   • PERIPHERAL VIA PERIPHERAL VEIN
  • 12. BLOOD TEST PRIOR TO EXCHANGE  BIOCHEMISTRY  FULL SEPTIC WORKUP  ON CORD BLOOD:  DIRECT COOMBS TEST  HB  SERUM BILIRUBIN  ON BABYS BLOOD.  ABO, RH FACTOR, DIRECT COOMBS TEST
  • 13. TYPES OF BLOOD NEEDED  • O Rh –ive blood is used   • If available before delivery, cross match against mothers blood   • If obtained after delivery ,cross match with infants blood
  • 14. AMOUNT OF BLOOD FOR DOUBLE EXCHANGE  85* wt *2   This removes 85% of infants rbcs   At end of exchange bilirubin should be about 50% of pre   exchange level
  • 15. BASELINE OBSERVATION  • Vital signs   • Blood sugar level   • Abdominal girth measurement to evaluate haemorrhage   • Urine analysis   • Infants color tone activity
  • 16. PRINCIPLES  Carried through a catheter using a three way cannula  Blood is drawn out of baby 5-20ml and discarded down outflow line  Aliquots 5ml for 1kg, 10ml for 2kg,, 15ml for 3kg, >3kg 20ml cycles  Donor blood is warmed drawn into a syringe and injection slowly.
  • 17. PRINCIPAL  App 100ml/ 15min should be exchanged  Record exact amount of blood exchanged  Equal volumes exchanged in and out  Vital signs recorded every 15 mins
  • 18. RISK DURING EXCHANGE  Blood overload congestive heart failure  Insufficient blood anaemia  Perforation with catheter  Air or blood embolism
  • 19. COMPLICATION  Infection  Haemorrhage  Anaemia  Trauma to vessels  Arrhythmia and cardiac failure  Hypotension and shock  Electrolyte imbalance  Graft vs host disease
  • 20. VIDEO
  • 21. PHARMACOLOGICAL THERAPY  Phenobarbital  Action: Induce production of glucoronyltransferase and Increase bilirubin excretion  Indication: CNJ II syndrome and Gilbert syndrome  Dose: 2.5 mg/kg/day  Metalloporphyrins Synthetic heme ,inhibit heme oxygenase thus decrease the production of bilirubin
  • 22. PHARMACOLOGICAL THERAPY  Intravenous Albumin Given 1g/kg over 2 hours can provide more binding sites for free bilirubin  Iv immunoglobulin Block fc receptors in neonatal reticuloendothelial system and prevent further haemolysis is recommended if TSB is rising despite intensive phototherapy  Dose:500mg -1g/kg over 2hours  Repeated after 12 hours
  • 23. MANAGEMENT OF CONJUGATED BILIRUBIN  MEDICAL MANAGEMENT  Antibiotics (sepsis, UTI)  L-thyroxin (hypothyroidism)  Hormone replacement therapy  Vitamins  Dietary restriction
  • 24. PHARMACOLOGICAL THERAPY  Ursodiol  20 mg /kg /day in 2 divided doses  Phenobarbital  3-5mg/kg /day  Cholestyramin  Surgical management